A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534886



Internal ID310630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129144727..129144741hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534886
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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